Reduced expression of 15-hydroxy prostaglandin dehydrogenase in chorion during labor is associated with decreased PRB and increased PRA and GR expression

Am J Pathol. 2013 May;182(5):1585-94. doi: 10.1016/j.ajpath.2013.01.033. Epub 2013 Mar 15.

Abstract

The chorion laeve controls the levels of active prostaglandins within the uterus by NAD-dependent 15-hydroxy prostaglandin dehydrogenase (PGDH). The expression of PGDH in chorion is modulated by glucocorticoids and progesterone. In this study, we investigated glucocorticoid receptor (GR) and progesterone receptor A and B (PRA and PRB) in the regulation of PGDH expression in chorion, and we determined whether reduced PGDH expression in chorion during labor is associated with the changes in GR and PR expression by real-time RT-PCR and Western blot analysis. Dexamethasone (DEX) inhibited PGDH expression whereas progesterone stimulated PGDH expression in chorionic trophoblasts. DEX suppressed PGDH expression in GR overexpression and PR knockdown cells. The inhibitory effect of DEX did not occur in GR knockdown cells. Progesterone inhibited PGDH in GR overexpression and PR knockdown cells and it stimulated PGDH in PRB overexpression cells whereas it suppressed PGDH in PRA overexpression cells. Knockdown of c-Jun resulted in a loss of progesterone- and DEX-induced effects. PGDH was down-regulated in chorion tissues during labor. PRB was decreased whereas PRA and GR were increased in chorion during labor. Glucocorticoids inhibit PGDH expression via GR in chorionic trophoblasts. Progesterone enhances PGDH expression through PRB, whereas it inhibits PGDH expression via GR and PRA. Decreased PGDH expression is associated with increased GR and PRA, although decreased PRB, in chorion during labor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cells, Cultured
  • Chorion / cytology
  • Chorion / drug effects
  • Chorion / enzymology*
  • Dexamethasone / pharmacology
  • Dihydrotestosterone / analogs & derivatives
  • Dihydrotestosterone / pharmacology
  • Extraembryonic Membranes / drug effects
  • Extraembryonic Membranes / metabolism
  • Female
  • Fluorescent Antibody Technique
  • Glucocorticoids / pharmacology
  • Humans
  • Hydroxyprostaglandin Dehydrogenases / genetics
  • Hydroxyprostaglandin Dehydrogenases / metabolism*
  • Labor, Obstetric / drug effects
  • Labor, Obstetric / metabolism*
  • Pregnancy
  • Progesterone / pharmacology
  • Proto-Oncogene Proteins c-jun / metabolism
  • Receptors, Glucocorticoid / metabolism*
  • Receptors, Progesterone / metabolism*
  • Transcription, Genetic / drug effects
  • Trophoblasts / cytology
  • Trophoblasts / drug effects
  • Trophoblasts / metabolism
  • Up-Regulation / drug effects

Substances

  • Glucocorticoids
  • Proto-Oncogene Proteins c-jun
  • Receptors, Glucocorticoid
  • Receptors, Progesterone
  • progesterone receptor A
  • progesterone receptor B
  • Dihydrotestosterone
  • Progesterone
  • Dexamethasone
  • Hydroxyprostaglandin Dehydrogenases
  • trilostane